HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354572Generated: October 27, 2026
Acetyl chloride → 6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl Acetate
https://huagongshe.com/reaction/354572
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 6-(2,4-Dichlorophenyl)-4-hydroxy-5-hexene-2-one | HCID 54359312 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl Acetate | HCID 54467667 | 87.4% |
Reaction Steps
Acetyl chloride (1.2 ml, 16.5 mmole) was added dropwise to a stirred solution of 6-(2,4-dichlorophenyl)-4-hydroxy-5-hexene-2-one (3.9 g, 15 mmole) in pyridine (60 ml) at 0° C. The ice bath was removed, and the reaction mixture was stirred at 20° C. for 2 hours and then diluted with ether (300 ml). The ether solution was washed with 1 N HCl (3×300 ml) and saturated NaHCO3, dried over MgSO4, filtered and evaporated. The residual pale amber oil (4.1 g) was chromatographed on a 50 mm column with 15 cm of silica gel (230-400 mesh). Elution with methylene chloride (2 L) provided the title compound as a pale yellow oil (3.95 g, 87%): pmr (CDCl3) δ2.03 (3H, s), 2.17 (3H, s), 2.83 (2H, dd).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04375475 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-a8e5684d54fc4ed9846617a6e8fc6b01 |
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| Source note | uspto-grants-1983_03 |
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